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- W2000896073 endingPage "144" @default.
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- W2000896073 abstract "The central role K-, H- and N-Ras play in regulating diverse cellular pathways important for cell growth, differentiation and survival is well established. Dysregulation of Ras proteins by activating mutations, overexpression or upstream activation is common in human tumors. Of the Ras proteins, K-ras is the most frequently mutated and is therefore an attractive target for cancer therapy. The complexity of K-ras signaling presents many opportunities for therapeutic targeting. A number of different approaches aimed at abrogating K-ras activity have been explored in clinical trials. Several of the therapeutic agents tested have demonstrated clinical activity, supporting ongoing development of K-ras targeted therapies. However, many of the agents currently being evaluated have multiple targets and their antitumor effects may not be due to K-Ras inhibition. To date, no selective, specific inhibitor of K-ras is available for routine clinical use. In this review, we will summarize the structure and function of K-ras with attention to its role in tumorigenesis and discuss the successes and failures of the various strategies designed to therapeutically target this important oncogene." @default.
- W2000896073 created "2016-06-24" @default.
- W2000896073 creator A5041114807 @default.
- W2000896073 creator A5063434798 @default.
- W2000896073 date "2005-11-01" @default.
- W2000896073 modified "2023-10-17" @default.
- W2000896073 title "K-ras as a target for cancer therapy" @default.
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